Supamit Ukarapong

Assistant Professor of Clinical

  • 23 Citations
20122019
If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Dive into the research topics where Supamit Ukarapong is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Metabolic Bone Diseases Medicine & Life Sciences
Cholestasis Medicine & Life Sciences
Gonadal Dysgenesis Medicine & Life Sciences
Disorders of Sex Development Medicine & Life Sciences
Mutation Medicine & Life Sciences
Megakaryocytes Medicine & Life Sciences
Nephrotic Syndrome Medicine & Life Sciences
Premature Infants Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2012 2019

  • 23 Citations
  • 6 Article

Vitamin D status among preterm infants with cholestasis and metabolic bone disease

Ukarapong, S., Zegarra, W., Navarrete, C., Seeherunvong, T. & Berkovitz, G., Jan 1 2019, (Accepted/In press) In : Pediatric Research.

Research output: Contribution to journalArticle

Metabolic Bone Diseases
Cholestasis
Premature Infants
Vitamin D
Vitamin D Deficiency
8 Citations (Scopus)

Risk factors of metabolic bone disease of prematurity

Ukarapong, S., Venkatarayappa, S. K. B., Navarrete, C. & Berkovitz, G., Sep 1 2017, In : Early Human Development. 112, p. 29-34 6 p.

Research output: Contribution to journalArticle

Metabolic Bone Diseases
Cholestasis
Birth Weight
Parenteral Nutrition
Diuretics

Early recognition of gonadal dysgenesis in congenital nephrotic syndrome

Ukarapong, S., Berkovitz, G., McElreavey, K., Bashamboo, A. & Bao, Y., 2016, In : Clinical Nephrology. 86, 6, p. 341-344 4 p.

Research output: Contribution to journalArticle

Gonadal Dysgenesis
Nephrotic Syndrome
Mutation
Steroids
46,XY Gonadal Dysgenesis
2 Citations (Scopus)

Childhood hypophosphatasia with homozygous mutation of ALPL

Ukarapong, S., Ganapathy, S. S., Haidet, J. & Berkovitz, G., Jan 1 2014, In : Endocrine Practice. 20, 10, p. e198-e201

Research output: Contribution to journalArticle

Mutation
Knee
Hypophosphatasia
Genes
Phenotype
8 Citations (Scopus)

Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD

Seeherunvong, T., Ukarapong, S., McElreavey, K., Berkovitz, G. & Perera, E. M., Feb 1 2012, In : Journal of Pediatric Endocrinology and Metabolism. 25, 1-2, p. 121-123 3 p.

Research output: Contribution to journalArticle

Disorders of Sex Development
Testis
X Chromosome
Microsatellite Repeats
Genes